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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Covidien Auto Suture; LAPAROSCOPE, GENERAL & PLASTIC SURGERY

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Covidien Auto Suture; LAPAROSCOPE, GENERAL & PLASTIC SURGERY Back to Search Results
Model Number OMS-T12BT
Medical Device Problem Code Break (1069)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/06/2026
Type of Reportable Event Malfunction
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Brand Name
Auto Suture
Common Device Name
LAPAROSCOPE, GENERAL & PLASTIC SURGERY
Manufacturer (Section D)
Covidien
sabanetas industrial park
ponce PR 00716 -440
Manufacturer (Section G)
Covidien
sabanetas industrial park
ponce PR 00716 -440
Manufacturer Contact
mike bocchino
8200 coral sea st ne
mounds view, MN 55112--439
+1(800)646-4633
MDR Report Key50420813
Report Number2647580-2026-02535
Device Sequence Number16097870
Product Code GCJ
UDI-Device Identifier10884521081093
UDI-Public(01)10884521081093(17)280430(10)P5E1236(20)02
Combination Product (Y/N)N
Initial Reporter CountryTW
PMA/510(K) Number
K924011
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,Company Representative
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date (Section B) 08/24/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model NumberOMS-T12BT
Device Catalogue NumberOMS-T12BT
Device Lot NumberP5E1236
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date08/24/2026
Date Device Manufactured05/30/2025
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
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